Our Vision: A quality of life for people living with MND which is not compromised by their diagnosis - a life with dignity and independence.


The MND and Me Foundation Limited is a not for profit organisation that was formed to raise awareness of Motor Neurone Disease (MND) and its' impact in the community. We saw the desperate need to assist people living with MND and their families to maintain their independence and quality of life for as long as possible. The Foundation intends to contribute financially toward research into finding a cure, but until one is found, our major objectives are to ensure those who have to live with this terrible disease and their families are supported by the Foundation both in financial and non-financial ways.


Book Tickets Online Here!

Book Tickets Online Here!

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Latest News & Events

MND and Me Gala Dinner Tickets – NOW CLOSED!

MND and Me Gala Dinner Tickets – NOW CLOSED!

TICKETING IS NOW CLOSED!

The 2012 MND and Me Gala Dinner will be held on St. Patrick’s Day Saturday March 17t…
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ALS/MND Symposium, Sydney 2011 Overview by Dr. Rob Henderson

ALS/MND Symposium, Sydney 2011 Overview by Dr. Rob Henderson

Overview of the ALS/MND Symposium, Sydney 2011
by Dr. Rob Henderson (Neurologist – RBWH MND Clinic Brisbane)
What…
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2011 in Review – Raising Awareness

2011 in Review – Raising Awareness

The Foundation has been very active in seeking exposure on a local, state, national and international level in 2011…
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2011 in Review – Supporting Research

2011 in Review – Supporting Research

2011 has been an encouraging year for advancements in MND research. Recently Sydney hosted the International Sympos…
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Coming in 2012 – The MND and Me Foundation Grants Program

Coming in 2012 – The MND and Me Foundation Grants Program

In January we will be establishing the 2012 MND and Me Foundation Grants Program. The grants program will have a si…
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Coming in 2012 – The MND and Me Foundation Emotional Support Service

Coming in 2012 – The MND and Me Foundation Emotional Support Service

In January we will also establish a specialised MND counselling service available to all Queenlanders with MND. The…
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Who is Scott Sullivan?

Coming in 2012 – The MND and Me Foundation Emotional Support Service


Awarded 2011 Queensland ‘Pride of Australia Medal’ for Courage

Scott Sullivan is a 39 year old vibrant, fun-loving and energetic husband and father of two young children. On October 22, 2010 he was diagnosed with Motor Neurone Disease (MND) – a disease with no known cause, no known cure and no effective treatment. His life expectancy is 3-5 years.

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